HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474351Generated: October 29, 2026
Thioacetamide → Ethyl 2-methyl-4-(2-methylphenyl)-1,3-thiazole-5-carboxylate
https://huagongshe.com/reaction/474351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | 2-Bromo-3-oxo-3-o-tolyl-propionic acid ethyl ester | HCID 22437388 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-methyl-4-(2-methylphenyl)-1,3-thiazole-5-carboxylate | HCID 53440888 | 34% |
Reaction Steps
A stirred mixture of 2-bromo-3-oxo-3-o-tolyl-propionic acid ethyl ester (2.74 g, 9.60 mmol, 1.0 equiv) and thioacetamide (0.76 g, 10.1 mmol, 1.05 equiv) in ethanol (30 mL) was heated to reflux for 4 hours. The cooled mixture was filtered and concentrated under vacuum. The residue was partitioned between ethyl acetate and water and the organic phase was separated and then washed with saturated aqueous sodium chloride solution. The collected organic was dried over magnesium sulphate, filtered, and concentrated under vacuum. The resultant residue was purified by flash column chromatography on silica gel (gradient: 0 to 20% ethyl acetate in pentane) to afford 0.84 g (34%) of 2-methyl-4-o-tolyl-thiazole-5-carboxylic acid ethyl ester as an oil. LCMS (ESI) m+H=261.9; 1H NMR (400 MHz, CDCl3) δ: 7.31-7.18 (m, 4H), 4.16 (q, 2H), 2.76 (s, 3H), 2.18 (s, 3H), 1.14 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08637526B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-d8696266c6da46af8659fd8e3f03da8f |
|---|
| Source note | uspto-grants-2014_01 |
|---|